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Filtered Search Results
Medchemexpress LLC AZD9496 maleate | ≥95.0% | 2 MG
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AZD9496 maleate is a potent and selective estrogen receptor (ERα) antagonist. It acts as an orally bioavailable selective oestrogen receptor degrader (SERD).
- Potent and selective ERα antagonist
- Orally bioavailable selective oestrogen receptor degrader (SERD)
- IC50 of 0.28 nM
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eMolecules 103-60-6 | 2-Phenoxyethyl isobutyrate | Ambeed | MFCD00027363 | 208.257 | C12H16O3 | 98.000 | CC(C)C(=O)OCCOc1ccccc1 | 25g | 490489950
2-Phenoxyethyl isobutyrate | Ambeed | 103-60-6 | MFCD00027363 | 208.257 | C12H16O3 | 98.000 | CC(C)C(=O)OCCOc1ccccc1 | 25g | 490489950
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eMolecules 2090332-56-0 | methyl 1-amino-6-bromoisoquinoline-4-carboxylate | Synthonix281.109 | C11H9BrN2O2 | 95.000 | COC(=O)c1cnc(N)c2ccc(Br)cc12 | 250mg | 779537019
methyl 1-amino-6-bromoisoquinoline-4-carboxylate | Synthonix | 2090332-56-0281.109 | C11H9BrN2O2 | 95.000 | COC(=O)c1cnc(N)c2ccc(Br)cc12 | 250mg | 779537019
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eMolecules 53673-40-8 | 1-(2-AMINOETHYL)-3-ISOPROPYLUREA | AstaTech | MFCD09998224 | 145.206 | C6H15N3O | 95.000 | CC(C)NC(=O)NCCN | 1g | 112531466
1-(2-AMINOETHYL)-3-ISOPROPYLUREA | AstaTech | 53673-40-8 | MFCD09998224 | 145.206 | C6H15N3O | 95.000 | CC(C)NC(=O)NCCN | 1g | 112531466
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![Medchemexpress LLC Methyl 5-[benzylsulfonyl-...]-2-[(4-methylphenyl)methoxy]benzoate | 1919853-46-5 | MFCD31382181 | 99.9% | 680.79 | C34H36N2O9S2 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215068.png-250.jpg)
Medchemexpress LLC Methyl 5-[benzylsulfonyl-...]-2-[(4-methylphenyl)methoxy]benzoate | 1919853-46-5 | MFCD31382181 | 99.9% | 680.79 | C34H36N2O9S2 | 25 MG
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PTP1B-IN-2 is a potent small-molecule inhibitor of protein tyrosine phosphatase 1B (PTP1B) that potently inhibits the target (IC50 = 50 nM) and demonstrates cellular activity by enhancing insulin receptor β phosphorylation and increasing insulin-stimulated glucose uptake in muscle cells.
- Potent PTP1B inhibition (IC50 50 nM).
- High selectivity versus SHP-2 and LAR (>40-fold).
- Improved selectivity versus TCPTP (~15-fold).
- Enhances insulin-mediated IRβ phosphorylation in cells.
- Increases insulin-stimulated glucose uptake in L6 myotubes.
- High purity suitable for research use (≈99.9%).
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Selleck Chemical LLC Timolol Maleate S4123-50mg
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Timolol Maleate (MK-950 (S)-Timolol Maleate) is a non-selective beta-adrenergic receptor antagonist for 1/ 2 with Ki of 1 97 nM/2 0 nM
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Selleck Chemical LLC Indacaterol Maleate S3083-1g
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Indacaterol (QAB149) is an ultra-long-acting -adrenoceptor agonist with pKi of 7 36 for 1-adrenoceptor and pKi of 5 48 for 2-adrenoceptor
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Medchemexpress LLC Trimebutine (maleate) | 34140-59-5 | 99.7% | 1 ML
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Trimebutine (maleate) | 34140-59-5 | 99.7% | 1 ML
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TARGETMOL CHEMICALS INC FLUPIRTINE MALEATE 200MG
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Also available in 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Flupirtine maleate (Katadolon maleate) a centrally acting non-opioid analgesia is the salt form of Flupirtine. It is an NMDA receptor antagonist and also a specific neuronal potassium channel opener. purity: 99%
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Medchemexpress LLC Ciproxifan maleate | 184025-19-2 | C20H22N2O6 | 1 ML
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Ciproxifan maleate is a potent, selective, orally bioavailable, and competitive antagonist of the histamine H3-receptor, with an IC50 of 9.2 nM. It shows low apparent affinity at other receptor subtypes and can be used for the research of aging disorders and Alzheimer's disease.
- Inhibits [3H]HA release from synaptosomes of rat cerebral cortex (Ki: 0.5 nM).
- Inhibits binding of [125I]iodoproxyfan with rat striatal membranes (Ki: 0.7 nM).
- Increases t-MeHA level in mouse brain (ED50: 0.14 mg/kg).
- Improves accuracy of responding in five-choice tasks in rats.
- Induces neocortical electroencephalogram activation and waking state in cats.
- Decreases H3-receptor ligand concentration in serum in mice.
- Exhibits oral bioavailability (F=62%) and maximal concentration (Cmax=420 nM) in mice.
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Medchemexpress LLC (S)-timolol maleate | 26921-17-5 | MFCD00058356 | 100.0% | 432.49 | C17H28N4O7S | 10 MG
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(S)-Timolol maleate is the S-enantiomer of timolol supplied as the maleate salt and provided as an analytical/research standard for pharmacological testing, method development, and quality control. It is a non-cardioselective, hydrophilic β-adrenoceptor blocker commonly used in research related to intraocular pressure and cardiovascular effects.
- Analytical standard for method development and quality control.
- S-enantiomer maleate salt with defined stereochemistry.
- High purity suitable for HPLC and reference standard use.
- Molecular weight 432.49 and formula C17H28N4O7S.
- Store sealed at 4°C, protected from light and moisture.
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Medchemexpress LLC Avitinib maleate | 1557268-88-8 | 99.9% | 603.60 | 25 MG
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Avitinib maleate is a third-generation, irreversible, and orally active selective EGFR inhibitor. It has IC50 values of 0.18 nM against both EGFR L858R and EGFR T790M, and 7.68 nM against wild-type EGFR. It is also a BTK inhibitor, inducing apoptosis and inhibiting BTK phosphorylation in mantle cell lymphoma. It exhibits anticancer effects.
- Third-generation, irreversible, and orally active selective EGFR inhibitor.
- Potent against EGFR L858R, EGFR T790M, and wild-type EGFR.
- BTK inhibitor.
- Induces apoptosis.
- Inhibits phosphorylation of BTK in mantle cell lymphoma.
- Exhibits anticancer effects.
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Medchemexpress LLC Setiptiline maleate | 85650-57-3 | 99.9% | 377.43 | 50 MG
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Setiptiline maleate is a serotonin receptor antagonist and a tetracyclic antidepressant (TeCA) that acts as a noradrenergic and specific serotonergic antidepressant (NaSSA).
- Functions as a norepinephrine reuptake inhibitor.
- Acts as an α2-adrenergic receptor antagonist.
- Serves as a serotonin receptor antagonist, targeting 5-HT2A, 5-HT2C, and/or 5-HT3 subtypes.
- Acts as an H1 receptor inverse agonist/antihistamine.
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TARGETMOL CHEMICALS INC ACEPROMAZINE MALEATE 50MG
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Also available in 5 mg 10 mg 25 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ACEPROMAZINE MALEATE is a dopamine receptor antagonistpurity: 99%
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Medchemexpress LLC Way-100635 maleate | 1092679-51-0 | MFCD01321056 | 99.6% | 538.64 g/mol | C29H38N4O6 | 100 MG
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WAY-100635 maleate is the maleate salt of WAY-100635, a potent and selective 5-HT1A receptor antagonist used for pharmacology and receptor-binding research. It is provided as a high-purity analytical standard suitable for in vitro and in vivo studies.
- Potent 5-HT1A receptor antagonist (IC50 = 0.91 nM; Ki = 0.39 nM).
- High purity: 99.6% (HPLC).
- Molecular weight 538.64 g/mol.
- Molecular formula C29H38N4O6.
- Supplied as a 100 mg vial for research use.
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